HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262902Generated: October 30, 2026
Dimethyl Sulfoxide → N-1,2-benzisoxazol-3-yl-4-(4-phenyl-1,3-oxazol-2-yl)piperazine-1-carboxamide
https://huagongshe.com/reaction/2262902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(4-Phenyl-1,3-oxazol-2-yl)piperazine | HCID 68775735 | — |
| Reactant | Bis(2,2,2-trichloroethyl) 1,2-benzisoxazol-3-ylimidodicarbonate | HCID 86625471 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-1,2-benzisoxazol-3-yl-4-(4-phenyl-1,3-oxazol-2-yl)piperazine-1-carboxamide | HCID 68777876 | — |
Reaction Steps
A mixture of 1-(4-Phenyl-1,3-oxazol-2-yl)piperazine (391 mg, 0.807 mmol), bis(2,2,2-trichloroethyl) 1,2-benzisoxazol-3-ylimidodicarbonate (370 mg, 1.61 mmol), diisopropylethylamine (0.141 ml, 0.807 mmol) and dimethylsulfoxide (5 ml) was stirred at 70° C. for 2 hours. The reaction mixture was poured to water and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to give the desired product as a solid. The resulting solid was recrystallized from a mixed solvent of ethyl acetate and hexane to give 44.0 mg (14.1%) of the desired product. mp 171-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851473B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-9ae19a1ebc874e4193a4b0ba44e69f4c |
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| Source note | uspto-grants-2010_12 |
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